Proposed Data Collection Submitted for Public Comment and Recommendations, 20161-20163 [2021-07838]
Download as PDF
20161
Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses; and
5. Assess information collection costs.
Proposed Project
American Academy of Pediatrics
(AAP) Neurodevelopmental Extension
inform any needed changes in topics,
procedures, or other aspects of the
program. The purpose and use of the
session evaluation data will be to assure
that specific information is conveyed
and understood by participants for each
monthly session, ongoing improvement
in identification and referral by
participating pediatricians, and to
inform subsequent neurodevelopmental
ECHO projects.
Data will be collected through secure
email and will include monthly chart
reviews, a monthly session evaluation
survey, one overall program evaluation
survey at the end of the project period,
and one overall debriefing conference
call at the end of the project. The target
population is actively practicing
pediatricians. Quantitative descriptive
analyses are planned for the chart
reviews. Qualitive data will be obtained
from the session and program
evaluation surveys, as well as the
debriefing conference call. CDC requests
approval for an estimated 496
annualized burden hours.
for Community Health Outcomes
(ECHO) Program on Children with Fetal
Alcohol Spectrum Disorders (FASD)—
New—National Center on Birth Defects
and Developmental Disabilities
(NCBDDD), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The purpose of this information
collection is to monitor and evaluate the
American Academy of Pediatrics (AAP)
Neurodevelopmental Extension for
Community Health Outcomes (ECHO)
Program on Children with Fetal Alcohol
Spectrum Disorders (FASD). The intent
of the project is to improve practicing
pediatrician capacity for identification
and care of children with
neurodevelopmental disorders,
particularly prenatal exposure to
alcohol, in the medical home.
Evaluation information will be used
to monitor any incorporation of
presented materials or suggestions from
ECHO sessions into participating
pediatric practices. Feedback also will
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Pediatricians
Pediatricians
Pediatricians
Pediatricians
Number of
responses
Burden per
response
(minutes)
Burden in
hours
...............
...............
...............
...............
Chart Review ..........................................................
Session evaluation survey .....................................
Program evaluation survey ....................................
Debriefing conference call ......................................
15
15
15
15
160
8
1
1
12/60
5/60
5/60
60/60
480
10
1
15
Total .....................
.................................................................................
........................
........................
........................
496
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–07840 Filed 4–15–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–21–21EE; Docket No. CDC–2021–
0033]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Form name
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
SUMMARY:
VerDate Sep<11>2014
19:57 Apr 15, 2021
Jkt 253001
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Integrated Viral Hepatitis
Surveillance and Prevention Funding
for Health Departments. This new data
collection is for viral hepatitis (VH) case
reporting data collected from the
National Notifiable Diseases
Surveillance System (NNDSS) which
provides the primary population-based
data used to describe the epidemiology
of VH in the United States and for
annual reporting of surveillance,
prevention, and epidemiology
performance measures via an Annual
Performance Report.
CDC must receive written
comments on or before June 15, 2021.
DATES:
PO 00000
Frm 00048
Fmt 4703
Sfmt 4703
You may submit comments,
identified by Docket No. CDC–2021–
0033 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
ADDRESSES:
E:\FR\FM\16APN1.SGM
16APN1
20162
Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7118; Email: omb@cdc.gov.
Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses; and
5. Assess information collection costs.
SUPPLEMENTARY INFORMATION:
Proposed Project
jbell on DSKJLSW7X2PROD with NOTICES
Integrated Viral Hepatitis Surveillance
and Prevention Funding for Health
Departments—New—National Center
for HIV/AIDS, Viral Hepatitis, STD, and
TB Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
VerDate Sep<11>2014
19:57 Apr 15, 2021
Jkt 253001
Background and Brief Description
CDC is authorized under Sections 304
and 306 of the Public Health Service Act
(42 U.S.C. 242b and 242k) to collect
information on cases of viral hepatitis
(VH). Data collected by the National
Notifiable Diseases Surveillance System
(NNDSS) are the primary data used to
monitor the extent and characteristics of
the VH burden in the United States. VH
surveillance data are used to describe
trends in VH incidence, prevalence, and
characteristics of infected persons and
are used widely at the federal, state, and
local levels for planning and evaluating
prevention programs and health-care
services, and to allocate funding for
prevention and care.
In 2021, CDC is implementing
activities under a new cooperative
agreement Integrated Viral Hepatitis
Surveillance and Prevention Funding
for Health Departments (CDC–RFA–
PS21–2103). Tools exist to prevent new
cases of hepatitis A, B, and C, to treat
people living with hepatitis B, and to
cure people living with hepatitis C. Yet
new cases of VH continue to rise, many
people infected with VH remain
undiagnosed, and far too many VHrelated deaths occur in the US each
year. The purpose of the activities under
a new cooperative agreement is to
enable states to collect data to evaluate
disease burden and trends and to
analyze and disseminate that data to
develop or refine recommendations,
policies, and practices that will
ultimately reduce the burden of VH in
their jurisdictions. The goals of the
activities are to reduce new VH
infections, VH-related morbidity and
mortality, and VH-related disparities
and to establish comprehensive national
VH surveillance, which are in
accordance with the Division of Viral
Hepatitis 2025 Strategic Plan.
The activities of the new cooperative
agreement are separated into two
components (Component 1:
Surveillance, and Component 2:
Prevention), containing six strategies:
1.1, develop, implement, and maintain
a plan to rapidly detect and respond to
outbreaks for hepatitis A, B, and C; 1.2,
collect, analyze, interpret, and
disseminate data to characterize trends,
and implement public health
interventions for hepatitis A, acute
PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
hepatitis B and acute and chronic
hepatitis C; 1.3 (contingent on available
funding), collect, analyze, interpret, and
disseminate data to characterize trends
and implement public health
interventions for chronic hepatitis B and
perinatal hepatitis C; 2.1, support VH
elimination planning and surveillance,
and maximize access to testing,
treatment, and prevention; 2.2
(contingent on available funding),
increase access to HCV and HBV testing
and referral to care in high-impact
settings; and 2.3 (contingent on
available funding), improve access to
services preventing VH among persons
who inject drugs. Contingent on
funding, an optional component
(Component 3: Special Projects) will
support improved access to prevention,
diagnosis, and treatment of viral,
bacterial and fungal infections related to
drug use in settings disproportionately
affected by drug use.
Performance measures will be
monitored to assess recipient
performance, including quality of data,
effective program implementation, and
accountability of funds. Data collection
via the Annual Performance Report is
used for program accountability and to
inform performance improvement.
Outbreak reporting will also be
submitted throughout the year. These
data, which complement case data as
another key component of national viral
hepatitis surveillance, are critical to
determining both the level of viral
hepatitis activity within a jurisdiction as
well as the effectiveness of each
jurisdiction’s approach to cluster and
outbreak response.
A standardized Case Report Form will
be used for surveillance data collection
submitted to the National Notifiable
Diseases Surveillance System (NNDSS).
De-identified data, including national
VH surveillance data, will be submitted
to CDC electronically per each
jurisdiction’s usual mechanism.
Recipients will submit other required
quantitative and qualitative
performance measure data annually via
an Annual Performance Report and as
needed for outbreak reporting. CDC
requests approval for an estimated 6,688
annual burden hours. There are no other
costs to respondents other than their
time.
E:\FR\FM\16APN1.SGM
16APN1
20163
Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Health
Health
Health
Health
Health
Health
Departments
Departments
Departments
Departments
Departments
Departments
Average
burden per
response
(in hours)
Total annual
burden
(in hours)
......
......
......
......
......
......
Viral Hepatitis Case Report Form ........................
APR: Component 1 ..............................................
APR: Component 2 ..............................................
APR: Component 3 ..............................................
Initial Outbreak Report Form ...............................
Outbreak Summary Report Form ........................
51
59
59
14
59
59
381
1
1
1
2
2
20/60
1
1
1
20/60
20/60
6,477
59
59
14
39
39
Total .......................
..............................................................................
........................
........................
........................
6,688
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–07838 Filed 4–15–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket No. CDC–2021–0042]
Advisory Committee on Immunization
Practices (ACIP)
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of meeting and request
for comment.
AGENCY:
In accordance with the
Federal Advisory Committee Act, the
Centers for Disease Control and
Prevention (CDC), announces the
following meeting of the Advisory
Committee on Immunization Practices
(ACIP). This meeting is open to the
public. The meeting will be webcast live
via the World Wide Web.
DATES: The meeting will be held on
April 14, 2021, from 1:30 p.m. to 4:30
p.m., EDT (dates and times subject to
change, see the ACIP website for
updates: https://www.cdc.gov/vaccines/
acip/). Written comments
must be received on or before April 16,
2021.
ADDRESSES: For more information on
ACIP please visit the ACIP website:
https://www.cdc.gov/vaccines/acip/
index.html.You may submit comments,
identified by Docket No. CDC–2021–
0042 by any of the following methods:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Centers for Disease Control
and Prevention, 1600 Clifton Road NE,
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Form name
VerDate Sep<11>2014
19:57 Apr 15, 2021
Jkt 253001
MS H24–8, Atlanta, GA 30329–4027,
Attn: April 14, 2021 ACIP Meeting
Instructions: All submissions received
must include the Agency name and
Docket Number. All relevant comments
received in conformance with the
https://www.regulations.gov suitability
policy will be posted without change to
https://www.regulations.gov, including
any personal information provided. For
access to the docket to read background
documents or comments received, go to
https://www.regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Stephanie Thomas, ACIP Committee
Management Specialist, Centers for
Disease Control and Prevention,
National Center for Immunization and
Respiratory Diseases, 1600 Clifton Road
NE, MS–H24–8, Atlanta, GA 30329–
4027; Telephone: 404–639–8367; Email:
ACIP@cdc.gov.
SUPPLEMENTARY INFORMATION: In
accordance with 41 CFR 102–3.150(b),
less than 15 calendar days’ notice is
being given for this meeting due to the
exceptional circumstances of the
COVID–19 pandemic and rapidly
evolving COVID–19 vaccine
development and regulatory processes.
The Secretary of Health and Human
Services has determined that COVID–19
is a Public Health Emergency. A notice
of this ACIP meeting has also been
posted on CDC’s ACIP website at: https://
www.cdc.gov/vaccines/acip/.
In addition, CDC has sent notice of this
ACIP meeting by email to those who
subscribe to receive email updates about
ACIP.
PURPOSE: The committee is charged
with advising the Director, CDC, on the
use of immunizing agents. In addition,
under 42 U.S.C. 1396s, the committee is
mandated to establish and periodically
review and, as appropriate, revise the
list of vaccines for administration to
vaccine-eligible children through the
Vaccines for Children (VFC) program,
along with schedules regarding dosing
interval, dosage, and contraindications
to administration of vaccines. Further,
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
under provisions of the Affordable Care
Act, section 2713 of the Public Health
Service Act, immunization
recommendations of the ACIP that have
been approved by the Director of the
Centers for Disease Control and
Prevention and appear on CDC
immunization schedules must be
covered by applicable health plans.
MATTERS TO BE CONSIDERED: The
agenda will include discussions on
Janssen (Johnson & Johnson) COVID–19
Vaccine Safety. A recommendation
vote(s) is scheduled. Agenda items are
subject to change as priorities dictate.
For more information on the meeting
agenda visit https://www.cdc.gov/
vaccines/acip/meetings/meetingsinfo.html.
Meeting Information: The meeting
will be webcast live via the World Wide
Web; for more information on ACIP
please visit the ACIP website: https://
www.cdc.gov/vaccines/acip/.
Public Participation
Interested persons or organizations
are invited to participate by submitting
written views, recommendations, and
data. Please note that comments
received, including attachments and
other supporting materials, are part of
the public record and are subject to
public disclosure. Comments will be
posted on https://www.regulations.gov.
Therefore, do not include any
information in your comment or
supporting materials that you consider
confidential or inappropriate for public
disclosure. If you include your name,
contact information, or other
information that identifies you in the
body of your comments, that
information will be on public display.
CDC will review all submissions and
may choose to redact, or withhold,
submissions containing private or
proprietary information such as Social
Security numbers, medical information,
inappropriate language, or duplicate/
near duplicate examples of a mass-mail
campaign. CDC will carefully consider
all comments submitted into the docket.
E:\FR\FM\16APN1.SGM
16APN1
Agencies
[Federal Register Volume 86, Number 72 (Friday, April 16, 2021)]
[Notices]
[Pages 20161-20163]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-07838]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-21-21EE; Docket No. CDC-2021-0033]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled Integrated Viral Hepatitis
Surveillance and Prevention Funding for Health Departments. This new
data collection is for viral hepatitis (VH) case reporting data
collected from the National Notifiable Diseases Surveillance System
(NNDSS) which provides the primary population-based data used to
describe the epidemiology of VH in the United States and for annual
reporting of surveillance, prevention, and epidemiology performance
measures via an Annual Performance Report.
DATES: CDC must receive written comments on or before June 15, 2021.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0033 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and
[[Page 20162]]
Prevention, 1600 Clifton Road NE, MS-D74, Atlanta, Georgia 30329;
phone: 404-639-7118; Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses; and
5. Assess information collection costs.
Proposed Project
Integrated Viral Hepatitis Surveillance and Prevention Funding for
Health Departments--New--National Center for HIV/AIDS, Viral Hepatitis,
STD, and TB Prevention (NCHHSTP), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC is authorized under Sections 304 and 306 of the Public Health
Service Act (42 U.S.C. 242b and 242k) to collect information on cases
of viral hepatitis (VH). Data collected by the National Notifiable
Diseases Surveillance System (NNDSS) are the primary data used to
monitor the extent and characteristics of the VH burden in the United
States. VH surveillance data are used to describe trends in VH
incidence, prevalence, and characteristics of infected persons and are
used widely at the federal, state, and local levels for planning and
evaluating prevention programs and health-care services, and to
allocate funding for prevention and care.
In 2021, CDC is implementing activities under a new cooperative
agreement Integrated Viral Hepatitis Surveillance and Prevention
Funding for Health Departments (CDC-RFA-PS21-2103). Tools exist to
prevent new cases of hepatitis A, B, and C, to treat people living with
hepatitis B, and to cure people living with hepatitis C. Yet new cases
of VH continue to rise, many people infected with VH remain
undiagnosed, and far too many VH-related deaths occur in the US each
year. The purpose of the activities under a new cooperative agreement
is to enable states to collect data to evaluate disease burden and
trends and to analyze and disseminate that data to develop or refine
recommendations, policies, and practices that will ultimately reduce
the burden of VH in their jurisdictions. The goals of the activities
are to reduce new VH infections, VH-related morbidity and mortality,
and VH-related disparities and to establish comprehensive national VH
surveillance, which are in accordance with the Division of Viral
Hepatitis 2025 Strategic Plan.
The activities of the new cooperative agreement are separated into
two components (Component 1: Surveillance, and Component 2:
Prevention), containing six strategies: 1.1, develop, implement, and
maintain a plan to rapidly detect and respond to outbreaks for
hepatitis A, B, and C; 1.2, collect, analyze, interpret, and
disseminate data to characterize trends, and implement public health
interventions for hepatitis A, acute hepatitis B and acute and chronic
hepatitis C; 1.3 (contingent on available funding), collect, analyze,
interpret, and disseminate data to characterize trends and implement
public health interventions for chronic hepatitis B and perinatal
hepatitis C; 2.1, support VH elimination planning and surveillance, and
maximize access to testing, treatment, and prevention; 2.2 (contingent
on available funding), increase access to HCV and HBV testing and
referral to care in high-impact settings; and 2.3 (contingent on
available funding), improve access to services preventing VH among
persons who inject drugs. Contingent on funding, an optional component
(Component 3: Special Projects) will support improved access to
prevention, diagnosis, and treatment of viral, bacterial and fungal
infections related to drug use in settings disproportionately affected
by drug use.
Performance measures will be monitored to assess recipient
performance, including quality of data, effective program
implementation, and accountability of funds. Data collection via the
Annual Performance Report is used for program accountability and to
inform performance improvement.
Outbreak reporting will also be submitted throughout the year.
These data, which complement case data as another key component of
national viral hepatitis surveillance, are critical to determining both
the level of viral hepatitis activity within a jurisdiction as well as
the effectiveness of each jurisdiction's approach to cluster and
outbreak response.
A standardized Case Report Form will be used for surveillance data
collection submitted to the National Notifiable Diseases Surveillance
System (NNDSS). De-identified data, including national VH surveillance
data, will be submitted to CDC electronically per each jurisdiction's
usual mechanism. Recipients will submit other required quantitative and
qualitative performance measure data annually via an Annual Performance
Report and as needed for outbreak reporting. CDC requests approval for
an estimated 6,688 annual burden hours. There are no other costs to
respondents other than their time.
[[Page 20163]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total annual
Type of respondent Form name respondents responses per response (in burden (in
respondent hours) hours)
----------------------------------------------------------------------------------------------------------------
Health Departments............ Viral Hepatitis 51 381 20/60 6,477
Case Report
Form.
Health Departments............ APR: Component 1 59 1 1 59
Health Departments............ APR: Component 2 59 1 1 59
Health Departments............ APR: Component 3 14 1 1 14
Health Departments............ Initial Outbreak 59 2 20/60 39
Report Form.
Health Departments............ Outbreak Summary 59 2 20/60 39
Report Form.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 6,688
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-07838 Filed 4-15-21; 8:45 am]
BILLING CODE 4163-18-P